US20040141637A1

Movatterモバイル変換

Info

Publication number: US20040141637A1
Application number: US10/752,072
Authority: US
Inventors: James Bacus
Original assignee: Bacus Laboratories Inc
Current assignee: Evident Scientific Inc
Priority date: 1996-08-23
Filing date: 2004-01-05
Publication date: 2004-07-22
Anticipated expiration: 2016-08-23
Also published as: US7542596B2; EP1252604A1; US7149332B2; US6674881B2; US7856131B2; US6396941B1; EP1252604A4; CA2398736A1; US8306298B2; CA2398736C; US20110145755A1; US20020135678A1; US20090210809A1; US20060188137A1; AU2001229630A1; WO2001054052A1; HK1049723A1

Abstract

A method of and apparatus for viewing microscopic images include transmitting tiled microscopic images from a server to a client. The client assembles the tiled images into a seamless virtual slide or specimen image and provides tools for manipulating image magnification and viewpoint. The method and apparatus also provides a virtual multi-headed microscope function which allows scattered viewers to simultaneously view and interact with a coherent magnified microscopic image.

Description

CROSS REFERENCE TO RELATED APPLICATIONS

This is a continuation of prior U.S. patent application Ser. No. 09/592,561, filed Jun. 12, 2000, which is hereby incorporated by reference in its entirety. This application claims the benefit of U.S. Provisional Patent Application No. 60/177,550, filed Jan. 21, 2000, U.S. patent application Ser. No. 09/592,561, now U.S. Pat. No. 6,396,941 which is a continuation-in-part of U.S. patent application Ser. No. 09/032,514 filed Feb. 27, 1998, which is a continuation-in-part of U.S. patent application Ser. No. 08/805,856 filed Mar. 3, 1997, now U.S. Pat. No. 6,101,265, which is a continuation-in-part of U.S. patent application Ser. No. 08/701,974 filed Aug. 23, 1996, now U.S. Pat. No. 6,031,930.[0001]

BACKGROUND OF THE INVENTION

The invention relates to a method of and an apparatus for storing and viewing virtual microscope slides. The method and apparatus are usable over the Internet, an intranet, or on a local computer, and provide an integrated and interlocked combination of a digital image server and multiple virtual microscope client viewers.[0002]

Examination of tissue sections, aspirated tissue, and the like, has typically been a localized activity. That is, the tissue is sectioned in a lab. It may be stained and microscopically examined by a light microscope after which a technician and/or a pathologist reaches a conclusion as to the characteristics of the tissue; for instance whether the tissue is benign or malignant and what stage of malignancy the tissue might be in. A number of patents awarded to the instant inventors are directed to that sort of system.[0003]

In some cases, however, it may be desirable where results are indefinite or where particular sophistication is needed for the human analysis of the images to be able to supply the slides to an offsite expert who might be across the country or on the other side of the world. In the past, the approach which has been taken to solve this problem has involved the transfer of the slides themselves by air express or post, often involving significant time delays which it would be desirable to avoid if a patient is suspected of being severely ill.[0004]

In the alternative, telepathology systems have been made available involving the use of television transmissions requiring a 6 MHz bandwidth, either through a satellite link or possibly through a coaxial cable, both of which must, in effect, be dedicated lines and previously set up. Such a system, however, requires a great deal of customization and expense although such systems do include the use of computer-controlled microscopes. Such microscopes receive commands from a remote location to move to a particular position on a slide so that the television camera may send a television signal out representative of the field of view.[0005]

This type of system is relatively expensive and clumsy to use do to the necessity for a very expensive robotically-controlled microscope which receives specialized signals over a dedicated link.[0006]

What is needed then is a system and apparatus which can allow a remote consult to take place related to tissue specimens, and the like, which may be done quickly, conveniently, and easily.[0007]

SUMMARY OF THE INVENTION

The invention relates to a method for viewing virtual microscope slides. Virtual microscope slides comprise sets of tiled images. The tiles of the tiled images represent a field of view which may be captured from a microscope having a high-precision controlled stage typically with a stage resolution in the neighborhood of a. {fraction (1/10)}th micron step. The images are captured on a CCD array which generates images in color or black and white and stores them in a frame buffer or on disk in tiled format. Such images are usually very large due to the number of pixels required to reproduce a substantial size tissue specimen at a high magnification, such as 40 power. In addition, in order to provide ease of use, particularly on a remote basis, other sets of tiled images have a lower magnification, for instance at 1.25 power. All of the images are tiled and stored in digital format on a server which may communicate using the hypertext transport protocol used for web-based communications over a packet switching network such as the Internet or an intranet. Because the images have already been captured and coordinated in tiled form, it is unnecessary to provide a robotically-controlled microscope or even the original specimens themselves.[0008]

One or more clients may communicate with the server containing the image to download a portion or all of the tiled image. The client provides requests to the server indicating the portion which is desired to be viewed and the server supplies the appropriate tiles for that portion of the image. The tiles are received by the client and are assembled into a seamless view which may be scrolled through and scanned in the same manner as a pathologist may move about a microscope slide to find regions of interest. In addition, the low-magnification image may be displayed in a first window at the client and a higher-magnification image may simultaneously be displayed which retains coherence with the lower-magnification image in order to provide ease of scanning for areas of interest by the pathology, or the like.[0009]

Furthermore, the client/server relationship may be carried out over multiple clients with one of the clients having control over the image positioning as fed by the server for all other clients via communication between the first client and the server, and then subsequent updating coherent communication between the server and the downstream clients. This does not necessarily require that repeated loading take place of the client images, but only that signals be sent between the server and the secondary clients reflecting the field which the first client is viewing. In this way, the overall system can operate similarly to a multiheaded optical microscope of the type used to train physicians in pathology. Furthermore, the system can be used as a multiheaded microscope during a consult so that al persons simultaneously involved in the consult are looking at the same portion of the image and no confusion can arise.[0010]

A further advantage of the present invention is to provide packet switched chat communications along with the multiheaded virtual microscope feature to allow text to be transferred among the various clients while the images are being viewed.[0011]

Finally, additional lines of communication may be provided among the users of the multiple remote client locations so that they can discuss telephonically or even using a voice-over-Internet protocol-based system to confer in real time on the images that are being seen at each of the client stations.[0012]

Furthermore, the client in control of the image may relinquish control to a second client; the first client operating on a peer basis with the other clients in a secondary relationship thereafter.[0013]

In order to provide further analysis features, a linear measuring or tape measuring feature may be provided in order to determine the distance in microns, or the like, between a pair of points identified by pointing and clicking on portions of the image in order to determine the actual size of particular features shown in the specimen image. The size, of course, is computed on the basis of the magnification of the image being shown.[0014]

Other objects and advantages of the present invention will become obvious to one of ordinary skill in the art upon a perusal of the following specification and claims in light of the accompanying drawings.[0015]

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a block diagram of a system according to the invention for creating and transmitting locally, over an intranet or via the Internet data structures of an image of specimen on a microscope slide;[0016]

FIG. 1A is representation of a microscope slide which has been arbitrarily assigned to be scanned into eighty tiled images;[0017]

FIG. 1B is a representation of the detected signals of the individual pixel sensors in a CCD optical array after detecting a selected image area to tile and the referenced data files containing the information describing the detected signals;[0018]

FIG. 2 is a screen view of a system embodying the present invention showing a low magnification image of a specimen on a microscope slide in one window, a high magnification image of a portion of the low magnification image selected by a region marker and a control window;[0019]

FIG. 3 is a view of a display screen of the apparatus embodying the present invention showing the control window a low magnification window having a plurality of high magnification micro image regions delineated therein and a high magnification window including one or more of the micro image regions;[0020]

FIG. 4 is a view of a macro image of an actual breast cancer specimen displayed at 1.25× as seen on a computer monitor;[0021]

FIG. 5 is a view of the grid portion of FIG. 4 outlining a region of interest selected by a pathologist displayed at 40× magnification;[0022]

FIG. 6 is a block diagram of the steps in the mapping of the scanned image from the optical sensor array to computer bit map in memory to the display on a user's monitor;[0023]

FIG. 7A is a file listing such as would be seen under Windows 95 file manager showing the data files included in a data structure for a breast cancer specimen;[0024]

FIG. 7B is a file listing of a Java applet for controlling a data structure;[0025]

FIG. 8 is file listing such as would be seen under Windows 95 file manager showing the data files included in an alternate data structure for a breast cancer specimen;[0026]

FIGS. 9A and 9B are a block diagram of the apparatus embodying the present invention;[0027]

FIG. 10 is a block diagram of a portion of the apparatus shown in FIG. 9 showing details of a mechanical arrangement of a microscope;[0028]

FIG. 11 is a flow diagram related to operation of the apparatus;[0029]

FIG. 12 is a flow diagram of details of one of the steps in FIG. 11;[0030]

FIG. 13 is a display screen showing control parameters to be manipulated thereon;[0031]

FIG. 14 is a flow chart for a region outlying routine;[0032]

FIG. 15 is a flow chart for a scanning and analyzing routine;[0033]

FIG. 16 is a schematic showing of the limits of travel of the microscope stage with respect to the image tiles;[0034]

FIG. 16A is a perspective view of the microscope stage and stepper motors and encoders providing a closed loop drive for the motors;[0035]

FIG. 17 is a block diagram of a networked system allowing multiple workstations to obtain access to the microscope and to manipulate the microscope locally at each workstation;[0036]

FIG. 17A is a view of the system described in connection with FIG. 10;[0037]

FIG. 18 is a block diagram of a remote networked system for distributing and accessing diagnostic images and data, i.e. virtual microscope slides, through a hypertext transport protocol based server directly or over a packet network;[0038]

FIG. 19 shows a system having interlinking and an integrated combination of image viewer and server concept using an Internet or intranet connection embodying the present invention;[0039]

FIG. 20 shows a server comprising a portion of the system shown in FIG. 19 and functioning as a listening socket to respond to GET requests and create event threads in a simultaneous multi-threaded operating environment;[0040]

FIG. 21 shows logic to determine valid GET requests;[0041]

FIG. 22A shows an interaction between a thin client browser program and the Internet or intranet server computer with a server program as shown in FIG. 20;[0042]

FIG. 22B shows an HTML-embedded Java applet viewer window for a client subsystem of the system shown in FIG. 19;[0043]

FIG. 23 shows an interaction between a Java applet program and Internet or intranet servers executing a server program and embodying the present invention;[0044]

FIG. 24 shows a thin client browser main window upon initial activation of the thin client browser shown in FIG. 22A;[0045]

FIG. 25 shows a main window with a Slide Tray tab activated, showing available images from a remote server;[0046]

FIG. 26 shows a selection in the tray holding slide name Prost-z1 and showing a thumbnail image of a virtual slide together with associated identification information;[0047]

FIG. 27 shows a main window of the thin client browser showing a tab after selection of a virtual slide for detailed viewing in response to the Slide Tray tab;[0048]

FIG. 28 shows a Slide View window chosen by selecting a point on the browser main window thumbnail image, a Slide View image shows an overlay set of a tiled region from which one or more higher-magnification Field View images may be chosen;[0049]

FIG. 29 shows a Field View window chosen by selecting an image tile region of the Slide View window shown in FIG. 28 using a pointer;[0050]

FIG. 30 is a flow chart of a typical sequence of interactions to view an image;[0051]

FIG. 31 shows a Server tab, showing options for multiple client interaction;[0052]

FIG. 32 shows a right mouse click activated pop-up menu when a pointer is positioned on an x, y location in the image area;[0053]

FIG. 33 shows a pointer position after choosing a “Set the Pointer” option in the menu of FIG. 32;[0054]

FIG. 34 shows a flow chart for major steps in process of filling in display windows with tiles; and[0055]

FIG. 35 shows an HTML-embedded Java applet viewer window.[0056]

FIGS. 36A through 36D are flow charts showing the operation of a server and a plurality of clients connected to the server for performing a virtual multi-headed microscope task.[0057]

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Referring now to the drawings and especially to FIG. 1, a[0058]

system

10 according to the invention is shown therein for creating, and transmitting over an intranet or via the Internet a virtual microscope slide, i.e. interrelated data structures, which may or may not include display procedures, depicting at multiple resolutions, images of a specimen on a microscope slide. The system includes a microscope with a digital platform for supporting the microscope slide. Digital platform orstage11 has been specially calibrated to include a large number of increments for locating portions of specimen images with high precision. After calibration and initial registration ofstage11 in the microscope setup, amicroscope slide13 or other substrate with aspecimen13ato be scanned is placed onstage11.

For exemplary purposes, the creation of virtual microscope slide specimen according to the invention will be described with respect to a breast cancer specimen. The first step in creating a data structure according to the invention is to establish a macro image of the entire specimen (or that portion of the specimen desired to be stored as the macro image). The purpose for creating the macro or large area thumbnail image is to enable the viewer to see the entire specimen at once and to use the entire image to choose those significant portions thereon for viewing at greater magnification. In this example, the user has selected 1.25× as the magnification to display the entire breast cancer slide. Once[0059]

specimen

13ahas been placed onstage11, rotatingoptical assembly15 are rotated to selectlens17 which corresponds to the 1.25× magnification.

In accordance with the teachings of the prior patent application, the computer controlled microscope is moved to scan the entire image of[0060]

specimen

13a. The focusing system is programmed to step through increments which detect/select only the high resolution center area of the field of view in order to avoid storing the blurred areas at the periphery of the field of view. In this example, the macro image will be stored in a 10 by 8 array, for a total of 80 contiguous image tiles, as shown in FIG. 1A.

A typical microscope slide is about 77 mm by 25 mm, where the usable area, without including the label, is about 57 mm by 25 m. Each of the 80 image segments is about 4.8 mm by 3.5 mm in dimension. This means each of the 80 image segments will be scanned separately and stored as a separate image tile.[0061]

The precision of the microscope systems is set up so that each step of the motor has a precision of 0.1 micron (micrometer). In this example, the microscope is set up to move 48,143 steps in the X direction and 35,800 steps in the Y direction at 1.25× magnification for each of the 80 image areas. At higher magnifications, the image areas to be scanned are considerably smaller, so the number of steps is corresponding smaller. For each of the 80 image areas, the microscope lens will detect only the high resolution center area of the field of view.[0062]

The optical image from the desired image area is then detected by an[0063]

optical array sensor

19, which preferably is a CCD sensor array. In this embodiment each of the 80 scanned areas is sensed by theentire array19, which includes 752 pixels by 480 pixels. Theoptical array sensor19 sends electrical signals indicative of the detected image to a microscope-controlledcomputer32. Thecomputer32 stores the scanned images, including the top left X-Y stage coordinates for each of the 80 individual areas of the microscope slide. Each of the 80 scanned image areas' pixel locations are stored in a bit-mapped file (i.e., a file which contains a map of the location of each bit in the area) which corresponds to the layout of the individual images thereon. Thus, all of the pixels from the image tile derived from region A on FIG. 1A, which is the seventh from the left and in the top row, are individually assigned unique locations in the computer memory's bit-mapped file (FIG. 6), and are also stored in the data structure image tile file as shown in FIG. 1B.

Each of the stored data image tiles is a standard image file with extension .bmp, and is of the order of one megabyte, i.e. each of the 752×480 pixels is stored as 3 bytes of red, green and blue image data (752×480×32=1,082,880 bytes). Since the location of each image tile is known according to the bitmap, the complete microscope image can be recreated by painting (displaying) each image tile in accordance with its grid location.[0064]

To display the resulting image, the[0065]

computer

32 calculates the appropriate portion to be displayed from each image tile depending upon the relative size of the display screen. Since the stored image data is usually greater than the size of the typical monitor, the viewer must scroll through the image on the window to view it entirely. However, an optional compression algorithm can be used to compress the entire image into the viewing window. The X-Y coordinate information is used by the viewing and manipulation program to reconstruct the image tiles into a complete image of the specimen. The resulting image is larger, and with better resolution than would be achieved if optics technology were able to construct a single lens capable of viewing the entire specimen in one field of view. In this example, each of the 80 image tiles has digital resolution of 752×480 pixels, with corresponding optical resolution of approximate 0.2 microns at 40× to approximately 6.4 microns at 1.25×.

After the macro or thumbnail images are digitally scanned and stored with their X-Y coordinate information, the user then examines the macro image or original specimen for significant details. Typically, the user will highlight with a marking pen the areas to be viewed at higher magnification. The user then changes the magnification of[0066]

optics system

15 to the desired higher magnification, moves the scanning system to bring the selected region into view. Thecomputer32 then repeats the scanning and image tile creation process for the selected region, but at higher magnification and with a new grid system to locate the scanned selected regions.

In the preferred embodiment example, the user has selected region B shown on FIG. 1A to perform a second view at a higher magnification. For example the user selects a 40× magnification. The[0067]

computer

32 calculates the number of tiles needed to fill the selected area at 40× magnification and sets up a second grid.

It should be noted that region B crosses over several of the larger tiles in FIG. 1A. Because of the extremely precise 0.1 micron resolution of the instrument, locating such selected regions with high resolution is readily accomplished. As noted above, the[0068]

computer

32 calculates the size of the image portion, in this case as an example, X=1500 and Y=1200 stepping increments. Each image portion at the 40× resolution is detected by the optical sensor array, 752 by 480 pixels. Each resulting data file is stored in a separate, high magnification mapped area of memory so that the computer can easily recall the location of region B, or any of its 200 individual image tiles, when requested by a user.

Once the user has completed selecting and having the computer controlled microscope system scan and store the digital images in image tiles, the[0069]

computer

32 stores the mapped .bmp files along with their coordinate information and creates the slideimage data structure31 shown in FIG. 1. Slideimage data structure31 includes all of the bit-mapped image tile files at both magnifications (note that similarly, additional images could be stored at further magnifications, if desired), as well as X-Y coordinate information for the location of the various image tiles.

FIG. 7A is a file listing such as would be seen under a Windows 95 file manager showing the data files included in a data structure for a breast cancer specimen. Included in the file listing are FinalScan.ini and SlideScan.ini as well as sixty bit-mapped data files. Slidescan.ini is a listing of all the original bit-mapped (.bmp) files. The bit-mapped files represent the individual image tiles in the scan at, say, 1.25× magnifications. Slidescan.ini is set forth below in Table 1 and describes the X-Y coordinates for each image tile file. When the data structure is viewed by a control program, the program uses the X-Y coordinates to display all the image tiles contiguously.[0070]

TABLE 1


Slidescan.ini

	[Header]
	x=278000
	y=142500
	lXStepSize=48143
	lYStepSize=35800
	iScannedCount=37
	[Ss1]
	x=181714
	y=142500
	[Ss2]
	x=133571
	y=142500
	[Ss3]
	x=37285
	y=106700
	[Ss4]
	x=85428
	y=106700
	[Ss5]
	x=133571
	y=106700
	[Ss6]
	x=181714
	y=106700
	[Ss7]
	x=229857
	y=106700
	[Ss8]
	x=229857
	y=70900
	[Ss9]
	X=181714
	y=70900
	[Ss10]
	x=133571
	y=70900
	[Ss11]
	x=85428
	y=70900
	[Ss12]
	x=37285
	y=70900
	[Ss13]
	x=−10858
	y=70900
	[Ss14]
	x=−10858
	y=35100
	[Ss15]
	x=37285
	y=35100
	[Ss16]
	x=85428
	y=35100
	[Ss17]
	x=133571
	y=35100
	[Ss18]
	X=181714
	y=35100
	[Ss19]
	x=229857
	y=35100
	[Ss20]
	x=278000
	y=−700
	[Ss21]
	x=229857
	y=−700
	[Ss22]
	x=181714
	y=−700
	[Ss23]
	x=133571
	y=−700
	[Ss24]
	x=85428
	y=−700
	[Ss25]
	x=37285
	y=−700
	[Ss26]
	x=−10858
	y=−700
	[Ss27]
	x=−10858
	y=−36500
	[Ss28]
	x=37285
	y=−36500
	[Ss29]
	x=85428
	y=−36500
	[Ss30]
	x=133571
	y=−36500
	[Ss31]
	x=181714
	y=−36500
	[Ss32]
	x=229857
	y=−36500
	[Ss33]
	x=278000
	y=−36500
	[Ss34]
	x=278000
	y=−72300
	[Ss35]
	x=229857
	y=−72300
	[Ss36]
	x=181714
	y=−72300
	[Ss37]
	x=133571
	y=−72300

Table 2 is a listing of the file FinalScan.ini, which is a listing the X-Y coordinates of the high magnification image tiles scanned and stored.[0071]

TABLE 2


FinalScan.ini

	[Header]
	tPatientID=mda027
	tAccession=
	tOperatorID=jwb
	tTimeOfScan=8/4/97 1:19:56
	PM
	lXStageRef=278000
	lYStageRef=142500
	iImageWidth=752
	iImageHeight=480
	lXStepSize=1590
	lYStepSize=1190
	lXOffset=−1900
	lYOffset=−400
	dMagnification=40
	lAnalysisImageCount=105
	lCalibrationImageCount=0
	[Da0]
	x=214532
	y=65584
	[Da1]
	x=212996
	y=65584
	[Da2]
	x=211460
	y=65584
	[Da3]
	x=209924
	y=65584
	[Da4]
	x=208388
	y=65584
	[Da5]
	x=206852
	y=65584
	[Da6]
	x=205316
	y=65584
	[Da7]
	x=203780
	y=65584
	[Da8]
	x=214532
	y=64400
	[Da9]
	x=212996
	y=64400
	[Da10]
	x=211460
	y=64400
	[Da11]
	x=209924
	y=64400
	[Da12]
	x=208388
	y=64400
	[Da13]
	x=206852
	y=64400
	[Da14]
	x=205316
	y=64400
	[Da15]
	x=203780
	y=64400
	[Da16]
	x=214532
	y=63216
	[Da17]
	x=212996
	y=63216
	[Da18]
	x=211460
	y=63216
	[Da19]
	x=209924
	y=63216
	[Da20]
	x=208388
	y=63216
	[Da21]
	x=206852
	y=63216
	[Da22]
	x=205316
	y=63216
	[Da23]
	x=203780
	y=63216
	[Da24]
	x=214532
	y=62032
	[Da25]
	x=212996
	y=62032
	[Da26]
	x=211460
	y=62032
	[Da27]
	x=209924
	y=62032
	[Da28]
	x=208388
	y=62032
	[Da29]
	x=206852
	y=62032
	[Da30]
	x=205316
	y=62032
	[Da31]
	x=203780
	y=62032
	[Da32]
	x=214632
	y=60848
	[Da33]
	x=212996
	y=60848
	[Da34]
	x=211460
	y=60848
	[Da35]
	x=209924
	y=60848
	[Da36]
	x=208388
	y=60848
	[Da37]
	x=206852
	y=60848
	[Da38]
	x=205316
	y=60848
	[Da39]
	x=203780
	y=60848
	[Da40]
	x=214532
	y=59664
	[Da41]
	x=212996
	y=59664
	[Da42]
	x=211460
	y=59664
	[Da43]
	x=209924
	y=59664
	[Da44]
	x=208388
	y=59664
	[Da45]
	x=206852
	y=59664
	[Da46]
	x=205316
	y=59664
	[Da47]
	x=203780
	y=59664
	[Da48]
	x=214532
	y=58480
	[Da49]
	x=212996
	y=58480
	[Da50]
	x=211460
	y=58480
	[Da51]
	x=209924
	y=58480
	[Da52]
	x=208388
	y=58480
	[Da53]
	x=206852
	y=58480
	[Da54]
	x=205316
	y=58480
	[Da55]
	x=203780
	y=58480
	[Da56]
	x=180740
	y=82160
	[Da57]
	x=179204
	y=82160
	[Da58]
	x=177668
	y=82160
	[Da59]
	x=176132
	y=82160
	[Da60]
	x=174596
	y=82160
	[Da61]
	x=173060
	y=82160
	[Da62]
	x=171524
	y=82160
	[Da63]
	x=180740
	y=80976
	[Da64]
	x=179204
	y=80976
	[Da65]
	x=177668
	y=80976
	[Da66]
	x=176132
	y=80976
	[Da67]
	x=174596
	y=80976
	[Da68]
	x=173060
	y=80976
	[Da69]
	X=171524
	y=80976
	[Da70]
	x=180740
	y=79792
	[Da71]
	x=179204
	y=79792
	[Da72]
	x=177668
	y=79792
	[Da73]
	x=176132
	y=79792
	[Da74]
	x=174596
	y=79792
	[Da75]
	x=173060
	y=79792
	[Da76]
	x=171524
	y=79792
	[Da77]
	x=180740
	y=78608
	[Da78]
	x=179204
	y=78608
	[Da79]
	x=177668
	y=78608
	[Da80]
	x=176132
	y=78608
	[Da81]
	x=174596
	y=78608
	[Da82]
	x=173060
	y=78608
	[Da83]
	x=171524
	y=78608
	[Da84]
	x=180740
	y=77424
	[Da85]
	x=179204
	y=77424
	[Da86]
	x=177668
	y=77424
	[Da87]
	x=176132
	y=77424
	[Da88]
	x=174596
	y=77424
	[Da89]
	x=173060
	y=77424
	[Da90]
	x=171524
	y=77424
	[Da91]
	x=180740
	y=76240
	[Da92]
	x=179204
	y=76240
	[Da93]
	x=177668
	y=76240
	[Da94]
	x=176132
	y=76240
	[Da95]
	x=174596
	y=76240
	[Da96]
	x=173060
	y=76240
	[Da97]
	x=171524
	y=76240
	[Da98]
	x=180740
	y=75056
	[Da99]
	x=179204
	y=75056
	[Da100]
	x=177668
	y=75056
	[Da101]
	x=176132
	y=75056
	[Da102]
	x=174596
	y=75056
	[Da103]
	x=173060
	y=15056
	[Da104]
	x=171524
	y=75056

[0072]

Computer

32 can also use the scanned image files to create a self-executing data structure. By compressing the .bmp images to .jpg and adding a dynamic, self-executing program which enables the user to view, reconstruct and manipulate the image tiles, the user can use the data structure as a virtual microscope slide of the original specimen. Preferably, the dynamic, self-executing program is a Java applet, such as shown on FIG. 7B.

[0073]

Computer

32 can provide the slideimage data structure31 directly or via anintranet browser33 tolocal viewer34, or via anInternet server38. Slideimage data structure37 is shown as being directly accessible fromInternet server38. Alternatively, a user can download the slide image data structure on hisown computer39, use aninternet browser43 and view the reconstructed images. Another alternative is forcomputer32 to store the slide image data structure on a CD-ROM, Jazz drive or other storage medium.

To view slide[0074]

image data structure

31 or37, the user, who for example, has acquired the data structure via a CD-ROM, first installs the CD-ROM in the CD-ROM drive of his computer. Then the user opens up a browser or other applications program which can read the Java applet installed on the CD-ROM with the image tiles. Note that in some instances no separate browser program may be required. In some case, the CD-ROM may include the complete applications program for viewing, reconstructing and manipulating the image tiles. In the instant example, the user will then select the icon or file listing for the slide image data structure and the control program will display the data files.

FIG. 2 is a screen view of a system embodying the present invention showing a[0075]

low magnification image

24 of a specimen on a microscope slide in one window, ahigh magnification image26 of a portion of the low magnification image selected by aregion marker30 and acontrol window28. FIG. 3 is a view of a display screen of the apparatus embodying the present invention showing thecontrol window28, alow magnification window24 having a plurality of high magnificationmicro image regions310 delineated therein and ahigh magnification window26 including one or more of the

micro image regions

310,314,316. FIG. 4 is a view of a macro image of an actual breast cancer specimen displayed at 1.25× as seen on a computer monitor. FIG. 5 is a view of the grid portion of FIG. 4 outlining a region of interest selected by a pathologist displayed at 40× magnification.

Recall that region A in FIG. 1A was about 4.8 mm by 3.5 mm. This area creates[0076]752 by 480 pixels of sensed data, or 360,930 pixels of information. Each pixel sends information about its location and the image it sensed to the computer. The computer stores this information in a series of data files (typically .bmp format, but .tif or .gif could also be used). Thus, it can be seen that several more pixels of sensed data are available for viewing on a computer monitor operating at 640 by 480. To view the entire image, the user must scroll through the image tiles. However, scrolling need not be done on a tile, by tile basis. Rather, the user scrolls by pointing to a pixel on the monitor.

FIG. 6 is a block diagram showing how the control program locates and scrolls through the stored image tiles. Using the example from FIG. 1[0077]a, a complete data structure has been created. When the user loads the data structure (of the microscope slide) into his personal computer or views it from an Internet browser, the control program recreates a bit map of the stored data. The bit map of the entire slide is shown in FIG. 6. Image tile A is also high-lighted. This bit map enables a user to point to or otherwise reference a location on the slide.

The X-Y coordinate information specified in the data structure enables X-Y translation of the specific image tiles and specific pixels within the image tile. When the control program first loads the image, because this image file is so large, only a small number of the available tiles are displayed in the active window on the user's monitor. The user uses his mouse or pointing device to scroll through the active window to view the entire macro image. The X-Y coordinate information selected by the mouse translates into specific image tiles or portions therein. The computer takes the mouse pointer information and retrieves the image data from the series of stored tile images and displays them on the monitor for viewing the by user.[0078]

Because of the large amount of CCD pixel information stored, actual CCD pixel information can be recreated in the viewing window. The entire system operates in a loop, where the user inputs a mouse location, the computer translates the mouse location from the screen coordinates (screen pixels) to the X-Y coordinates on the bit map.[0079]

As mentioned above, to save storage space,[0081]

computer

32 can perform a data compression on each of the image tile files. A preferred data compression is JPEG, which is readily transferred and recognized by most Internet browser programs. Also, JPEG allows flexibility in the amount of data to be compressed, from 20 to 80 percent. FIG. 8 is file listing such as would be seen under Windows 95 file manager showing the data files included in an alternate data structure, one in which the data files have been compressed or converted to JPEG (.jpg) format for a breast cancer specimen. The file index.html (shown in Table 3) is the listing which contains the X-Y coordinate information for these data files. This is the information that is read by the dynamic, self-executing program for viewing, reconstructing and manipulating the image tiles into the macro and micro views.

TABLE 3


index.html

<APPLET CODE=WebSlide/BliWebSlide.class NAME=DCIS_027

WIDTH=3384 HEIGHT=960 HSPACE=0 VSPACE=0 ALIGN=Middle>

</APPLET>

</BODY>

</HTML>

Referring now to the drawings, and especially to FIGS. 9A, 9B and[0082]10, apparatus for synthesizing low magnification and high magnification microscopic images is shown therein and generally identified byreference numeral10. The system includes acomputer12 which is a dual Pentium Pro personal computer in combination with a Hitachi HV-C20 video camera14 associated with aZeiss Axioplan 2microscope16. Thecomputer system12 is able to receive signals from thecamera14 which captures light from themicroscope16 having amicroscope slide10 positioned on an LUDL encodedmotorized stage20. The encodedmotorized stage20 includes a MAC 2000 stage controller for controlling the stage in response to thecomputer12. Amicroscope slide18 includes abiological specimen21 which is to be viewed by the microscope and whose image is to be digitized both at low magnification and at high magnification as selected by a user. The low magnification digitized image is then displayed on a 21 inch Iiyama video display monitor22 having resolution of 1600 by 1200 to provide display screens of the type shown in FIGS. 1 through 3 including alow magnification image24, for instance, at 1.25 power, ahigh magnification image26, for instance at 40× power and a control window orimage28. The low magnification image may have identified therein aregion30 which is reproduced at high magnification in high magnification screen orwindow26 so that a pathologist or other operator of the system can review architectural regions of interest inlow magnification image24 and simultaneously view them in high magnification in the high magnification screen orwindow26 to determine whether the cells forming a portion of the architectural feature need be examined further for cancer or the like or not.

The[0083]

computer

10 is constructed around aPCI system bus40 and has a first-Pentium Pro microprocessor42 and a second pentium promicroprocessor44 connected thereto. Thesystem bus40 has connected to it aPCI bus50 and anISA bus52. ThePCI bus50 has aSCSI controller60 connected thereto to send and receive information from ahard disk62. Thehard disk62′ also is coupled in daisy chain SCSI fashion to a high capacity removal disk and to aCD Rom drive66. Thehard disks62 contains the programs for operating the system for controlling themicroscope16 and for processing the images as well as for doing a quantitative analysis of the selected portions of the histological specimens being viewed on theslide18. Thesystem bus40 also has connected to it arandom access memory70 within which portions of the program being executed are stored as well as a read only memory72 for holding a bootstrap loader as well as portions of the basic input/output operating system. Afloppy disk controller74 is coupled to thesystem bus40 and has connected to it afloppy disk drive76 for reading and writing information to a floppy disk as appropriate. Amouse controller80 is coupled to the system bus and has amouse82 which operates as a pointing device for controlling manipulations on thescreen22 and within the

windows

24,26 and28. Akeyboard controller90 is connected to the system bus and has akeyboard92 connected thereto. Thekeyboard92 may be used to send and receive alpha numeric signals to other portions of the computer. Anaudio controller100 has a plurality of speakers102 and amicrophone104 connected thereto for audio input and output and is coupled to thesystem bus40. A network interface, such as anetwork interface card104, is connected to the system bus and can provide signals via achannel106 to other portions of a network or internet to which the system may be connected. Likewise, signals can be sent out of the system through amodem110 connected to theISA bus52 and may be sent via achannel112, for instance, to the internet. Aprinter116 is connected via a parallel I/O controller118 to the system bus in order to provide printouts as appropriate of screens and other information as it is generated. A serial I/O controller122 is connected to the system bus and has connected to it acamera controller124 which is coupled toCCD sensors126 in the cameras. TheCCD sensors126 supply pixel or image signals representative of what is found on theslide18 to an Epix pixciimage acquisition controller130 coupled to thePCI bus50.

The[0084]

microscope

16 includes a base140 having astage20 positioned thereon as well as anobjective turret142 having a plurality of

objectives

144,146 and148 thereon. The objective144, for instance, may be of 1.25× objective. The objective146 may be a 20× objective. The objective148 may be a 40× objective. Signals from the camera sensors and controller are supplied over abus128 to the image acquisition system where they are digitized and supplied to the PCI bus for storage in RAM or for backing storage on thehard disk62.

When a specimen is on the[0085]

slide

18 thestage20 may be manipulated under the control of the computer through astage controller160 coupled to the serial I/O controller122. Likewise, amicroscope controller162 controls aspects of the microscope such as the illumination, the color temperature or spectral output of alamp168 and the like. For instance, in normal operation, when a specimen is placed on the slide,specimen slide18 is placed on thestage20 in astep200, as shown in FIG. 14, the

processors

42 or44 send a command through the system bus to cause the serial I/O controller122 to signal the microscope controller to change magnification to 1.25× in astep202. This is done by rotating the objective turret of theAxioplan 2 microscope to select theobjective144. Likewise, the controller sets the color temperature of thelamp168, sets a pair of neutral

density filter wheels

170 and172 and sets afield diaphragm174 for the correct illumination. Acondenser diaphragm176 is also controlled and acolor filter wheel180 may also be controlled to apply the appropriate filter color to the CCD censors126 in the camera. The entire slide is then scanned in astep204. The images are tiled and melded together into theoverall image24 supplied on thescreen22 to provide the operator in thestep206 with a visually inspectable macro image of relevant regions of the slide of interest.

In order to provide the magnified image, the mouse may be moved to identify a marker segment or region which, for instance, may be a rectangular region which will cause the microscope to change magnification as at[0086]

step

208 to 4×, 20×, 40×, etc., by rotating the turret to bring the appropriate objective lens system into viewing position.

Next the user, in a[0087]

step

209a, uses the mouse to select the region on the macro image in order to select the micro image to be viewed on thescreen22. In astep209ba test is made to determine whether the user has commanded continued inspection. If the user has, a test is made in astep209cto determine if the magnification is to be changed by changing the selected objective. In the event the magnification is to be changed control is transferred to thestep208. If the magnification is to remain unchanged control is transferred to thestep209a. In the event inspection is not to continue the region selected is outlined for higher magnification scan in astep209d. In astep209e, a command may be received to scan or acquire the higher magnification image for display inscreen26. The image may then be archived for later analysis, displayed or analyzed immediately.

In order to perform the magnification called for in[0088]

step

206, the overall illumination and control of the microscope will be controlled so that in a step210 theobjective turret142 will be rotated to place the higher power objective above theslide18. In astep212 voltage to the lamp will be changed to adjust thelamp168 to provide the proper illumination and color temperature as predetermined for the selected objective. In a step214, thecondenser diaphragm176 will have its opening-selected as appropriate to provide the proper illumination for that objective. In astep216, thefilter turret180 will select the proper light wavelength filter to be supplied to the camera sensors. For instance, a red, blue or green filter, as appropriate, particularly if the specimen has been stained. In astep218 thefield diaphragm174 will have its opening changed. In astep220 the neutraldensity filter wheel170 will select a neutral density filter and in astep222 the neutraldensity filter wheel172 will also select a neutral density filter. In astep224 the X, Y and Z offsets will be used for reconstruction of the recorded image at the magnification and in astep226 the current position will be read from encoders in the stage which are accurate to 0.10 micron.

In order to identify the selected region the mouse is moved to that area of the region in a pointing operation in a[0089]

step

240 as shown in FIG. 14. The mouse may be moved to draw a box around the region selected. In astep242 the X and Y screen points are computed for the edges of the regions selected and the computed image or pixel points are translated to stage coordinate points in order to control the stage of the microscope. In a step244 a list of all of the X fields for positioning the stage for the objective is stored in random access memory and may be backed up on the hard disk. The information from the X offsets for the objective and the stage offsets is used as well as the size of the field to position the slide properly under the objective to capture the micro image.

When the slide has been positioned properly, as shown in FIG. 15 in a[0090]

step

250 the stage is positioned for each of the X and Y coordinate values in stage coordinate values and the digitized image is captured by the cameras and stored in RAM and backed up on the hard disk. The image may be then analyzed quantitatively in various manners such as those set forth in the previously-identified United States application. Optionally the image may be stored for archival purposes in astep254.

In order to override the specific control functions that take place as shown in FIG. 12, a screen is provided as shown in FIG. 13 wherein the X-Y step size can be edited, the X, Y and Z offset can be edited, the lamp voltage can be selected, the neutral density filter can be selected as well as the opening of the field diaphragm and several other microscopic characteristics. FIG. 13 is a view of the settings of the microscope objective properties of the[0091]Axioplan 2, computer-controlled microscope.

The X and Y positioning is specifically carried out as shown in FIG. 16 where the[0092]

slide

18 is shown with a

slide boundary

270,272,274 and276. Stage boundary for limits of the stage travel for purposes of the stage the stage can be moved all the way from an upper left hand corner oftravel276 to a lower right hand corner oftravel280. At the upper left hand bounded corner oftravel278 limits which a signal that the end of travel has been reached and the stage is then translated ashort distance282 in the extra action and ashort distance284 in the Y direction to define thefirst tile288 in terms of areference point290 at its upper left hand corner. Since the size of themacro image tile288 is known, the nextmacro image tile292 may be placed contiguous with it by moving the stage appropriately and by measuring the location of the stage from the stage in counters without the necessity of performing any image manipulation. The

image tiles

288 and292 may be abutted without any substantial overlap or they may be overlapped slightly, such as a one pixel with overlap, which is negligible insofar as blurring of any adjacent edges of abutted image tiles. The upperleft hand corner300 of thetile292 defines the rest of292 and other tiles can be so defined. Micro image tiles can likewise be defined so that they are contiguous but not substantially overlapping, as would interfere with the composite image. This avoids the problems encountered with having to perform extended computations on digital images in a frame storer or multiple frame storage in order to match or bring the images into contiguity without blurriness at the edges of contiguous image tiles. It may be appreciated that thelow power image24 has a plurality of micro images defined therein which are tiled and which are shown in higher magnification as

individual tiles

312,314,316 and the like. In addition, theregion310 when magnified as shown in thewindow26 may exceed the bounds of the window and thus the window may include scroll bars or other means for allowing theimage310 which is larger than thewindow26 to be examined from within thewindow26.

The[0093]

stage

200 is best seen in FIG. 16A and includes the X and

Y stepper motors

279 and281 with their respective encoders, which provide a closed loop system to give the 0.1 micron accuracy versus the usual 5 or 6 micron accuracy of most microscope stages without a closed loop system. This closed loop system and this very high accuracy allow the abutting of the tile images for both high magnification and low magnification images without the substantial overlap and the time-consuming and expensive software currently used to eliminate the overlap and blurriness at the overlapping edges of adjacent image tiles. With the precisely positioned stage and by using the tiling system described in connection with FIG. 16, where the slide is precisely positioned relative to a center point CP for the slide, and the known position ofpoint278 is always taken from the same point, the tiles may be positioned precisely in a horizontal row and precisely in vertical rows to reconstruct the macro image and the micro image. This reconstruction is done without the use, as in the prior art, of extensive software manipulation to eliminate overlapping image tiles, horizontally or vertically or the haphazard orientation of image tiles.

The present invention also includes the facility for allowing remote observation to occur by being able to couple the system either over a network communication facility to an intranet, for instance via the network interface, or via a modem or other suitable connection, to an internet so that once the image has been scanned and stored in memory or, hard disks or other storage, remote users may be able to access the low magnification image as well as the high magnification image and move around within both images to make determinations as to the histological characteristics of the samples.[0094]

An additional feature of the system includes a plurality of networked workstations coupled to a[0095]

first computer console

12 having adisplay screen22 connected to themicroscope14.

Satellite work stations

350 and352 are substantially identical to thework station12 including

respective computers

354 and356 coupled to

displays

358 and360. The devices can be manipulated throughinput devices360 and362 which may include a keyboard, mouse and the like. Also a third device can be connected including awork station370, having adisplay372, acomputer374 and aninput device376. Each of the devices is connected over

respective network lines

380,382,384 to thecomputer12 which transmission may be via either net or the like. Each of the different operators at the physically separate viewing stations can locate regions from the view of entire tissue cross sections via a macro view and label the regions for subsequent scanning and/or quantitative analysis. A single operator at theinstrument station12 can locate regions to view the entire tissue cross section. Those regions can be labeled for subsequent scanning and/or quantitative analysis with subsequent review and physically remote viewing stations, for instance, in an operating room or in individual pathologists' signout areas in order to review analysis results while still maintaining and reviewing the entire macro view of the tissue and/or the individual stored images from which the quantitative results were obtained. The

viewing stations

350,352 and370 can comprise desk top computers, laptops, etc. There is no need for a microscope at the

network stations

350,352 and370.

In a still further alternative embodiment,[0096]

remote workstations

400,402,404,406 and408 may be connected through aserver410 which may be supplied via a packet switched network. Theserver410 and may be a hypertext transport protocol based server of the type used for the World Wide Web or may be a telnet type server as used previously in internet remote operation applications. Theserver410 communicates via acommunications channel414 with alocal computer416 having adisplay418 associated therewith, thelocal computer416 being connected to theMicroscope420. Each of the

remote work stations

400,402,404,406 and408 may perform the same operations as the

stations

350,352 and370 although they do it from nearby buildings or even from around the world, thus providing additional flexibility for others to make use of the specimen obtained and being viewed under themicroscope420. In addition, stored images may be disseminated through theserver410 to theremote servers400 through408 for further analysis and review.

The server was designed to interact with either a thin client browser or with a Java applet viewer, operating through an HTML browser such as Netscape or the Microsoft Internet Explorer.[0097]

The server runs on a standard PC under a Windows operating system. It uses HTTP Internet communication protocols. The computer has stored on its storage media already collected data files having the data structure disclosed above. This data structure consists of “tiled” sets of digital images, with x, y information organized to aid the viewer program to “reconstruct” and spatially align physically-contiguous images, at multiple resolutions. The server responds to HTTP “Get” requests from multiple thin client browsers or other browsers with embedded Java applet viewers. As such, it uses a “listening socket” and a number of short-lived “threads” which handle “Get” requests independently and simultaneously, as shown in FIG. 28.[0098]

After initial logic, as shown in FIG. 29, to determine whether the HTTP request is valid and, if so, whether it is a Java request for a thin client request, the server generates a response thread, depending upon the request as detailed in Table 1, to send back the requested information to the client. Large numbers of these requests can be handled at one time.[0099]

The[0100]

server

12 was designed to interact with a client having either a thin client browser or with a Java applet viewer, operating through an HTML browser such as Netscape Navigator or Microsoft Internet Explorer.

The[0101]

server

12 runs on a standard PC under a Windows operating system. It uses the HTTP communication protocol. Thecomputer12 has stored on its storage media already collected data files of with the data structure disclosed in U.S. application Ser. No. 09/032,514, filed Feb. 27, 1998, which is incorporated herein by reference. This data structure consists of “tiled” sets of digital images, with x, y information organized to aid the viewer program to “reconstruct” and spatially align physically-contiguous images, at multiple resolutions. The server responds to HTTP “GET” requests from multiple thin client browsers or other browsers with embedded Java applet viewers. As such, it uses a “listening socket” and a number of short-lived “threads” which handle “GET” requests independently and simultaneously, as shown in FIG. 19.

After initial logic, as shown in FIG. 20, to determine whether the HTTP request is valid and, if so, whether it is a Java request or a thin client request, the server generates a response thread, depending upon the request as detailed in Table 4, to send back the requested information to the client. Large numbers of these requests can be handled at one time.[0102]

TABLE 4


Client - Server “GET” Interactions

Client Requests	Server Responses

Login Request	>	<	Acknowledges
User Name			Assigns and sends ID#
Nickname			to Client
E-mail address
Slide Tray Request	>	<	Sends Slide Tray Information
			List of image names and URL
			path locations on the server,
			extracted folder names and
			header text
Update Request	>	<	Sends same information to
User Name			requesting Client, for all
Nickname			of Clients currently logged
E-mail address			in, i.e., User Name,
Tray index			Nickname, etc.
Slide Name
Slide View Window
Information
Zoom Level
x, y position
Field View Window
Information
Zoom Level
x, y position
Action Status
Pointer Location x, y
Chat Buffer Index
Chat Line Request	>	<	Sends Chat Line message
ID#			string
Select Slide Request	>	<	Sends x, y coordinate
Modified URL Path			list for all tiles
of Selected Slide			associated with clients
			selected URL and the
			Preview Slide image.
Image Request	>	<	Send specified image,
			e.g., an image tile or
			thumbnail image
Logoff Request	>	<	Acknowledge
			Release User ID#
Java Applet Request	>	<	Send Java Applet
Java Login and Virtual	>	<	Send thumbnail and Preview
Slide Request			Images and x, y list of
Slide Name			title images
Verify Server Identity
Java Image Tile Request	>	<	Send requested image tile

In addition to the tiled image data, and the x, y coordinate lists for each tile of the image data, as set forth in Table 5 below there are several small reconstructed images that are stored in the individual folder, or on the server. These facilitate bringing image content to the client viewing screen rapidly, and can be used as an aid in determining what viewing options to choose in the various viewing programs.[0103]

TABLE 5


DA0	JPG	57,996	Da0.jpg
Da1	JPG	75,646	Da1.jpg
Da10	JPG	75,874	Da10.jpg
Da100	JPG	61,564	Da100.jpg
Da101	JPG	65,982	Da101.jpg
Da102	JPG	76,912	Da102.jpg
Da103	JPG	75,729	Da103.jpg
Da104	JPG	70,727	Da104.jpg
Da105	JPG	68,184	Da105.jpg
Da106	JPG	73,355	Da106.jpg
Da107	JPG	21,296	Da107.jpg
Da108	JPG	29,384	Da108.jpg
Da109	JPG	28,163	Da109.jpg
Da11	JPG	79,808	Da11.jpg
Da110	JPG	76,373	Da110.jpg
Da111	JPG	35,540	Da111.jpg
Da112	JPG	21,293	Da112.jpg
Da113	JPG	34,366	Da113.jpg
Da114	JPG	76,120	Da114.jpg
Da115	JPG	70,933	Da115.jpg
Da116	JPG	47,658	Da116.jpg
Da117	JPG	77,465	Da117.jpg
Da118	JPG	79,024	Da118.jpg
Da119	JPG	78,256	Da119.jpg
Da12	JPG	72,381	Da12.jpg
Da120	JPG	76,733	Da120.jpg
Da121	JPG	79,086	Da121.jpg
Da122	JPG	79,003	Da122.jpg
Da123	JPG	71,881	Da123.jpg
Da124	JPG	75,408	Da124.jpg
Da125	JPG	74,486	Da125.jpg
Da126	JPG	80,568	Da126.jpg
Da127	JPG	79,061	Da127.jpg
Da128	JPG	79,495	Da128.jpg
Da129	JPG	70,019	Da129.jpg
Da13	JPG	73,489	Da13.jpg
Da14	JPG	76,530	Da14.jpg
Da15	JPG	76,353	Da15.jpg
Da16	JPG	29,611	Da16.jpg
Da17	JPG	72,668	Da17.jpg
Da18	JPG	66,130	Da18.jpg
Da19	JPG	83,813	Da19.jpg
Da2	JPG	76,115	Da2.jpg
Da20	JPG	69/762	Da20.jpg
Da21	JPG	79,036	Da21.jpg
Da22	JPG	80,779	Da22.jpg
Da23	JPG	38,576	Da23.jpg
Da24	JPG	65,975	Da24.jpg
Da25	JPG	73,812	Da25.jpg
Da26	JPG	80,660	Da26.jpg
Da27	JPG	72,939	Da27.jpg
Da28	JPG	88,332	Da28.jpg
Da29	JPG	66,672	Da29.jpg
Da3	JPG	78,399	Da3.jpg
Da30	JPG	29,994	Da30.jpg
Da31	JPG	57,465	Da31.jpg
Da32	JPG	74,006	Da32.jpg
Da33	JPG	78,765	Da33.jpg
Da34	JPG	54,120	Da34.jpg
Da35	JPG	82,550	Da35.jpg
Da36	JPG	63,735	Da36.jpg
Da37	JPG	41,253	Da37.jpg
Da38	JPG	69,759.	Da38.jpg
Da39	JPG	49,376	Da39.jpg
Da4	JPG	77,922	Da4.jpg
Da40	JPG	52,514	Da40.jpg
Da41	JPG	68,291	Da41.jpg
Da42	JPG	69,726	Da42.jpg
Da43	JPG	79,840	Da43.jpg
Da44	JPG	80,526	Da44.jpg
Da45	JPG	84,245	Da45.jpg
Da46	JPG	50,315	Da46.jpg
Da47	JPG	73,069	Da47.jpg
Da48	JPG	73,188	Da48.jpg
Da49	JPG	69,155	Da49.jpg
Da5	JPG	69,257	Da5.jpg
Da50	JPG	69,087	Da50.jpg
Da51	JPG	74,156	Da51.jpg
Da52	JPG	82,847	Da52.jpg
Da53	JPG	74,838	Da53.jpg
Da54	JPG	69,003	Da54.jpg
Da55	JPG	73,524	Da55.jpg
Da56	JPG	65,242	Da56.jpg
Da57	JPG	67,796	Da57.jpg
Da58	JPG	70,367	Da58.jpg
Da59	JPG	39,998	Da59.jpg
Da6	JPG	68,210	Da6.jpg
Da60	JPG	14,487	Da60.jpg
Da61	JPG	76,801	Da61.jpg
Da62	JPG	74,394	Da62.jpg
Da63	JPG	69,446	Da63.jpg
Da64	JPG	63,296	Da64.jpg
Da65	JPG	17,568	Da65.jpg
Da66	JPG	71,935	Da66.jpg
Da67	JPG	71,736	Da67.jpg
Da68	JPG	67,406	Da68.jpg
Da69	JPG	74,488	Da69.jpg
Da7	JPG	69,660	Da7.jpg
Da70	JPG	45,382	Da70.jpg
Da71	JPG	69,849	Da71.jpg
Da72	JPG	12,009	Da72.jpg
Da73	JPG	62,862	Da73.jpg
Da74	JPG	68,522	Da74.jpg
Da75	JPG	67,734	Da75.jpg
Da76	JPG	60,510	Da76.jpg
Da77	JPG	26,689	Da77.jpg
Da78	JPG	68,839	Da78.jpg
Da79	JPG	67,137	Da79.jpg
Da8	JPG	71,914	Da8.jpg
Da80	JPG	65,232	Da80.jpg
Da81	JPG	78,365	Da81.jpg
Da82	JPG	63,535	Da82.jpg
Da83	JPG	74,889	Da83.jpg
Da84	JPG	71,895	Da84.jpg
Da85	JPG	65,744	Da85.jpg
Da86	JPG	76,849	Da86.jpg
Da87	JPG	74,373	Da87.jpg
Da88	JPG	73,449	Da88.jpg
Da89	JPG	69,255	Da89.jpg
Da9	JPG	74,054	Da9.jpg
Da90	JPG	65,637	Da90.jpg
Da91	JPG	62,566	Da91.jpg
Da92	JPG	75,703	Da92.jpg
Da93	JPG	70,315	Da93.jpg
Da94	JPG	63,884	Da94.jpg
Da95	JPG	62,949	Da95.jpg
Da96	JPG	69,046	Da96.jpg
Da97	JPG	77,595	Da97.jpg
Da98	JPG	71,528	Da98.jpg
Da99	JPG	58,862	Da99.jpg

Each image has a PreviewSlide.jpg image contained in its data structure. This is a “thumbnail” image reconstructed from all of the tiles from the low magnification, 1.25× slide view image tiles. The reconstructed composite image has been digitally reduced to an image size of 454×240. During server startup, for each data structure found as described below, this Preview Slide image is further converted to an additional thumbnail-image of 232×120. The use of the Preview Slide and thumbnail images will be described below. Also, if specific HTML Java applet views have been chosen, four reconstructed .jpg images from each view, corresponding to four different magnifications have also been stored on the server, as described in detail below under the Java applet creator description and image viewer descriptions.[0104]

FIGS. 21A, 21B and[0105]22 illustrate two different virtual microscope slide viewing implementations. These suit two different needs. The thin client browser has three screens and many more functions. As described in more detail below, there is a main screen that displays the thumbnail Preview Slide image, and uses a tabbed interface to implement different functionalities to the browser. Some of these important functionalities are: (1) a SlideTray tab, which allows for the selection of any of the stored images hosted on the server computer; (2) a server tab, which allows coordination of views and chats with multiple other clients all logged-in at the same time; and (3) an Applet Creation tab to select specific region views for HTML applets viewed by the Java Applet viewer. The other two windows, Slide View and Field View, allow viewing of low-magnification tiled images and high-magnification tiled images with scrolling and coordination between the two views.

The thin client browser is more suited to secondary opinion expert pathology consultations, and sophisticated professional pathology users in departmental pathology practice, for review of cases and as archival backup virtual slide records. In operation, the browser program is loaded separately, once on a client computer. After that it can be used to access any number of servers, as described below, by simply typing in the Internet address of the server. It is faster than the JAVA applets because it comprises code which is already compiled, and is not based upon interpreted applet execution. It is unnecessary to load the thin client browser for every virtual microscope slide viewed. During creation of the image, only smaller regions of specific diagnostic material need be scanned at high magnification, thus saving time during the scanning process.[0106]

The HTML applet viewer is simpler than the thin client browser, and may be used in medical student, dental student, veterinary and undergraduate biology teaching situations. Advantage is taken of the fact that most students are familiar with an HTML browser. Instructors can easily add course “content” text to provide different descriptions of the virtual microscope slide images. Since the virtual microscope slides will often be used for longer periods, and since there is no premium on speed of scanning, entire specimens can be scanned offline at high magnification which takes a longer time. In this viewer simply acts as a “portal,” or a small window, in a fixed position on a specific HTML page.[0107]

As described below, each applet instance relates to a specific image on a specific server computer. There are two parts to the view, the upper part of the portal is a display of the Preview Slide image. The bottom part of the portal initially shows a selected view from that image at one of four magnifications. A plurality of radio button choices loaded on a bar between the views allows for additional magnification choices in the bottom view. The bottom view is also scrollable, and can be changed by pointing the mouse to a region on the Preview Slide image.[0108]

It will-be appreciated that this viewer is simpler to learn initially and to operate than the thin client browser. It has the disadvantage of being slower and of only addressing one image at a time. It has an advantage of being simple, having various types of explanatory text right next to the image, and of being cross platform with regard to operating system, computer type and HTML browser type. These are all helpful in the educational market.[0109]

The Slide Tray-concept is used in the server and the browser programs and is central to providing an organizational construct to collections of images. It is set forth in Table 6 below.[0110]

TABLE 6


FINALS˜1	INI	3,902	FinalScan.ini
PREVIE˜1	JPG	6,210	PreviewSlide.jpg
SLIDES˜1	INI	654	SlideScan.ini
SS1	JPG	10,285	SS1.jpg
SS10	JPG	63,150	SS10.jpg
SS11	JPG	70,838	SS11.jpg
SS12	JPG	15,535	SS12.jpg
SS13	JPG	12,071	SS13.jpg
SS14	JPG	73,847	SS14.jpg
SS15	JPG	70,783	SS15.jpg
SS16	JPG	25,178	SS16.jpg
SS17	JPG	2,983	SS17.jpg
SS18	JPG	9,035	SS18.jpg
SS19	JPG	15,629	SS19.jpg
SS2	JPG	25,194	SS2.jpg
SS20	JPG	4,200	SS20.jpg
SS3	JPG	9,936	SS3.jpg
SS4	JPG	10,118	SS4.jpg
SS5	JPG	4,559	SS5.jpg
SS6	JPG	35,961	SS6.jpg
SS7	JPG	86,933	SS7.jpg
SS8	JPG	16,212	SS8.jpg
SS9	JPG	33,872	Ss9.jpg

	[Header]
	tPatientID=Prostate
	tAccession=
	tOperatorID=
	tTimeOfScan=9/17/98 4:56:31 PM
	lXStageRef=278000
	lYStageRef=142500
	iImageWidth=752
	iImageHeight=480
	lXStepSize=1588
	lYStepSize=1184
	lXOffset=0
	lYOffset=0
	dMagnification=40
	tImageType=.jpg
	iFinalImageQuality=60
	lAnalysisImageCount=130
	lCalibrationImageCount=0
	iiTotalBytes=9221691
	tFolder=Test WSTP
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It provides a flexible filing structure, whether the images are located in multiple places on a computer running a server program, or are collections held on removable storage media such as CD-ROMs and are just being viewed locally. The image data structure includes two modifiable text string byte arrays which are used to hold the file name and the folder name that identifies an individual image. When the server program is initiated, it searches all of its available storage (indicated in a setup file), finds any images present, reads the folder names and the file names of all of the images and creates URL path extensions for each one.[0111]

When the image browser initially starts its Main Window looks like FIG. 24. This is before a Login request has been initiated. The browser first sends a client Login Request using a specific server Internet address, such as shown in the address line of FIG. 20, and as indicated in Table 4. After the Login Request has been acknowledged, the browser then sends a Slide Tray Request. The server response to this is to send the list of image names and header text, their associated file folders, and the URL path extensions depending upon various image data structure storage locations on the server. The browser then constructs and displays in the Slide Tray tab of its main window a file folder tree structure display such as shown in FIG. 25. This is a dynamic display, such that a mouse click on the file folder opens up the file and displays its contained images. The browser responses are set forth in[0112]Tale 7 below.

TABLE 7


tResponse := tResponse + IntToStr0j0 + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tUserName + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tNickName + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tEmail + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tTrayIndex + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tSlide + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tSlideZoomLevel + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tSlideXRef + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tSlideYRef + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tFinalZoomLevel + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tXRef + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tYRef + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tSlideScanMode + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tPointerX + ‘&’;
tResponse := tResponse + FrmMain.Client[j].tPointerY + ‘&’;
if FrmMain.bLogoffClients then
tResponse := tResponse + ‘Server logoff issued...&’
else
tResponse := tResponse + FrmMain.Client[j].tStatus + ‘&’;
Inc(iCount);
end;
end;

A mouse click on a specific image file name activates a client Image Request to the server, and the server sends back the requested thumbnail image which is displayed in the tab image area, as shown in FIG. 25. If one of the virtual microscope images is of further interest for more detailed observation, it can be retrieved by further mouse clicks, either on the thumbnail image or by a double click on the Slide Tray tree structure file name. In this case, the client browser sends a Select Slide Request. As indicated in Table 1, the server then sends the larger Preview Slide image along with the x, y coordinate list of all image tiles associated with that virtual slide. The tab changes from the Slide Tray to the image tab and the Preview Slide image is displayed in the image display area, as shown in FIG. 26.[0113]

One of the advantages of this virtual slide tray organizational design is that the folder names are carried as part of the image data set structure. This is different from a standard file structure where the file name is created and files are moved into the created folder. In a virtual microscope slide environment, collections of slides may come from different sources, e.g., on CD-ROMs or other storage media. This method carries the file folder information with the slide. The server can then automatically organize, on startup, all of the file folders depending upon the media in place at that time. For read/write media, the folder names can be edited to put specific images into different folders. This method also allows for automatic folder generation during the image creation process, which reduces the possibility of mixup for collections of slides that go together.[0114]

As described above, the image data set is created initially by scanning the microscope slide at two different magnifications. The initial scan, which is referred to as the Slide View scan, is performed with a 1.25× objective lens and can potentially use as many as 8×10, or 80 tiles, to cover the region of tissue or cells deposited on the slide. The second, higher-magnification scan is referred to as the Field View scan, and can occupy variable regions. These regions are mapped to the Slide View regions, and can be shown as overlaid areas.[0115]

As shown in FIG. 22, there are a number of overlays in the image tab of the main image browser window that can be used as aids in navigating the images. Two of these are shown there. They indicate potential regions that could have been scanned and those that were actually scanned on the specimen. Clicking on one of these regions, using the mouse as a pointer, instructs the browser to bring up the Slide Scan window, as shown in FIG. 27. Depending upon the size of the Slide View window and the location point specified in the Preview Slide image, the browser program can use the x, y image list and associated URL information that was transferred in response to the Select Slide Request to determine which Slide View scan image tiles are necessary. The browser then issues an Image Request for each image tile and paints in the received tiles to fill in the image display area in the window.[0116]

There are optional navigation overlays for this window also. The illustrated overlay shows regions where higher-magnification image tiles exist in the image data structure. By clicking in the region of one of these tiles, the browser is instructed to bring up its third window, the Field View window, shown overlain on top of the other two windows in FIG. 28. It uses the same procedure, e.g., the size of the Field View window to determine which high-magnification image tiles to request. The size of the Field View and Slide View windows can be changed to suit the user, for example, to fill the available viewing screen, and the browser program will request and fill in the necessary tiles to fill the viewing area.[0117]

A number of other viewing options are available, including changing the digital image magnification, i.e., lowering from 40× to 5×. In this case, more tiles are requested to fill in the available viewing area. The combination of the ability to change the various windows position and size, and the digital magnification (zoom) allows for full inspection of the virtual microscope specimen at high and low magnifications throughout the entire specimen. As additional image tiles are requested, they are cached locally so that additional inspection becomes quicker.[0118]

FIG. 29 is a flow chart of typical usage to further illustrate the above. This flow chart is shown as a sequence of related steps since some should occur before others and this is a typical sequence. However, it should be appreciated that the browser is multi-threaded as well as event driven. Most of the time, for example, the Update Request process is running on its own thread concurrently with client user event-driven processes, a shown in FIG. 29.[0119]

Referring back to FIGS. 18 and 19, Table 4 and the server description, it is clear that multiple clients can be logged-in at one time. All such clients independently view the same or different images. The design of the total combined system or all components is more powerful than that, however, through the use of the Update Request indicated in Table 1. Update Requests are generated by each user logged in the client browser at one-second intervals. Through the use of these Update Requests, the server is essentially functioning as a total system “state machine” for all of the logged-in users. Since each user is assigned an ID number upon login, the server can pass information regarding all of the other logged-in users, with regard to which slide they are viewing, where on that slide they are looking, the status of any pointer locations, etc. This all happens at one-second intervals for all logged-in clients. The browser then can use this information if desired to view the same images seen by other clients. This essentially means that the network of client viewers operates as a virtual multi-headed microscope, letting each other simultaneously view the same virtual slide.[0120]

Additional features of the browser, as shown in FIG. 30, enhance this capability. The server tab in the main browser window, shown in FIG. 30, is used to activate a multi-headed virtual microscope function. A browser logged onto a server initially displays only the current user's information in the server tab. As Update Requests are serviced, if additional clients log onto the same server that information is also displayed in the Server tab, using additional login lines.[0121]

FIG. 30 shows two users logged into the same server. Also shown are buttons “Display another's view” and “Sync with another's view.” After point and click highlighting of one of the logged-in user lines, the current user can then, for example, click on the button “Display another's view” and the browser will use the last update information on that user to send a Select Slide Request, and whatever Image Tile requests are necessary to display the same image view that the user is looking at. In a similar manner, if the user clicked on “Sync with another's view,” then the browser would continue to use the update requests to change fields, zoom levels, etc. In the meantime, the various clients involved could communicate through the chat screen about the specimen under consideration.[0122]

As shown in FIG. 28, a pointer may be drawn at any x, y location on an image screen view. A right click mouse event on an image where the pointer is desired activates program code which creates a pop-up menu, as shown in FIG. 31. When the “Set the Pointer” menu option is chosen, the position of the pointer is computed in x, y stage coordinate units and those position values are put in the main window Pointer tab and kept in memory to pass along to the server on the next update. Also, a pointer is placed on the image, as shown in FIG. 32. when another client, logged on at the same time, activates “Display another's view” (as shown in FIG. 30) for the client displaying the pointer, then that second client's browser would use the Update Request transferred x, y pointer position from the first client to put a pointer on the second client's image, after any Image Requests to the server were satisfied. In this way, two clients can pass arrows back and forth.[0123]

This is additionally facilitated by the right click mouse menu that each can use when she has the same image in front of her. Usually, this occurs when both parties are on the telephone, using the Internet and talking to each other while they move pointers back and forth, or synchronize on each other's views as desired.[0124]

They can also communicate through the Chat process using the Server tab, as shown in FIG. 28, or through e-mail through the Server tab. It should be appreciated that more than two clients may be logged on and participate in this process. This provides a multi-headed virtual microscope environment with pointers for multiple client users simultaneously.[0125]

One of the most important technological improvements in the “tiling” methodology is the improved resolution of image capture and display compared to previous methods of capturing images and transferring them over the Internet. The reason for this relates to microscopy optical resolution compared to digital camera sensor resolution, and the limited “field of view” imposed by the aperture sizes of the microscopy system. In order to match the optical resolution to the digital sensor resolution at high magnification with readily-available sensors, only a small part of the specimen can be captured at one time. Attempting to capture a larger view, e.g., with a lower magnification (and as a result lower optical resolution) objective microscope lens onto digital camera sensor, and then digitally magnifying the resulting captured image, results in “pixelated,” “false” magnification. Tiled images can be captured at a matching pixel and optical resolution, and displayed seamlessly by the present invention, to achieve true virtual images. The same method automatically overcomes the limited “field of view” issue to preserve high resolution over large areas in the original high-magnification image plane of the microscope specimen.[0126]

The method of retrieving and displaying these tiles as a coherent connected image is depicted in the flow diagram of FIG. 33. This flow diagram is relevant for choosing by a point and click, an image point in the Preview Slide image of the main browser window to open and display the Slide View window (or to choose another region to display in an already open Slide View window), or to open and display at a higher magnification the Field View window from a point in the Slide View window, or to display image areas not already pre-loaded in the Java applet portal window in an HTML browser page. An important factor in accomplishing seamless tiled image display according to the methods of this invention is to maintain an image x, y pixel reference to the original mechanical stage x, y coordinate reference. In the preferred embodiment, the x, y stage resolution is 0.1 micrometers per step. Each image tile is a known number of pixels, in this instance 752×480 pixels. Through calibration setup procedures during instrument construction, the number of stage coordinate steps per pixel is determined. This varies slightly from system to system and is different for each microscope objective. It is therefore recorded as part of each image data set. Table 8 shows some typical examples of one system.[0127]

TABLE 8


Example Stage x, y Coordinates per Image Tile Pixel

		Pixel Spatial
	.1 Micrometer Stage	Resolution
Objectives	Steps Per Pixel	In Micrometers

1.25×	69	6.9
10×	9	.9
20×	5	.5
40×	2	.2

Using the values from Table 8, if a Slide View image data set consisted of a full component of 8×10 image tiles, then there would be 7,520 pixels along the x direction and 3,840 pixels in the y direction. This would result in an x, y coordinate system for this slide of 518,880 x coordinate values and 264,960 y coordinate values. This, in effect, creates a virtual coordinate reference system for each tiled image data set. As each tile is collected, the initial upper left starting pixel location in stage coordinate values is stored in a separate subfile list as part of the image data structure file, along with, of course, that .jpg tile image. They are associated with each other by the name of the image tile being used as the name in the list associated with the x, y coordinates. In this way, each data structure has contained in it a list of x, y coordinate positions. The x, y coordinate position list is transferred to a specific client in response to the client issuing a Select Slide Request.[0128]

Referring again to FIG. 33, the initial step is to translate the starting display image size in pixels into the virtual stage coordinates. For example, if the image is the 452×240 Preview Slide image then each x pixel increments by 1,148× virtual stage coordinates and each y pixel increments by 1,104 virtual stage coordinates. A given mouse click resulting in an x, y pixel location can then be easily translated into a known virtual image x, y location. Next, the new display image window, in this case the Slide View image, is opened, and some of the possible 8×10 1.25× image tiles may be displayed. This window will either have a present initial size or will have been set by a previous call. In either case the size of the window in pixels can be determined from the associated windows properties parameters, accessible to the program. The size and placement of this window can then be calculated in the virtual coordinate space. The program assumes that the pixel point chosen in the previous window is associated with the center of the new window to do this.[0129]

Next, the image stage coordinate list is searched. The image stage coordinate list was previously transferred to find all candidate tilts which should be displayed according to size of the window.[0130]

As shown in FIG. 33, the tiles can be two types; they may already have been viewed and are there, and are therefore cached and available locally, or they exist on the server. If they are on the server, a Send Image Request is initiated and the server sends back the requested tile. Otherwise, they are read from the cache. It should be appreciated again in the case of the program's execution, shown in the flow chart of FIG. 33, that the program is event driven and multi-threaded. The final operation is to fill in the display window with the chosen tile. This same, or an analogous method of filling in tiles for display images is used in scrolling, zooming in and out, and in retrieving tiles for the Field View window (coming from the Slide View window), and in retrieving image tiles from the server for the fixed size Java applet viewer.[0131]

Even though in many instances these five images would be sufficient, the additional approach of this invention is to make available to the applet, the entire virtual slide. This is accomplished using the techniques already described for the browser. In this instance, the upper panel Preview Slide Image can be used by a mouse point and click, to locate an x, y position. This is translated into x, y virtual stage coordinates, and the needed tiles are requested through an Image Request to the server. If the magnification choices are used the operation of this application is handled by the same methods of zoom and calling for images as in the browser, all relating to the size of the window and which image tiles are needed from what virtual x, y location to fill in the window. In a similar way, the lower portion of the portal window is also enabled for scrolling. So the virtual slide advantage of scrolling and zooming in and out are available but in a limited size window. They are accessible, however, from an HTML document that has embedded content.[0132]

An additional feature of this approach, as shown by comparing FIGS. 21A, 21B and[0133]22, is that the controlling HTML web-page code may be calling the content for the page from a computer other than the image computer. The advantage of this is that it decouples the text content from the image collections. In a teaching environment this enables many different users to create their own course content, using standard HTML methods, and simply provides a call to the server at appropriate places in the HTML code.

As indicated in FIGS. 18 and 19, and as discussed previously, the server also interacts with a second type of viewer, an HTML embedded applet, in this case written in the Java programming language, as set forth in Table 9 below.[0134]

TABLE 9


<APPLET CODEBASE=“http://209.100.40.94/” CODE=“WebSlide”
ALIGN=“m
iddle” HEIGHT=“590” NAME=“Histology06a” WIDTH=“464”
ALT=“WebSlide”>
<PARAM NAME=“lslidexrefpos” VALUE=“82458”>
<PARAM NAME=“webslideurl”
VALUE=“http://209.100.40.94/WebSlides/
Histology06a/”>
<PARAM NAME=“izoomlevel” VALUE=“2”>
<PARAM NAME=“lyrefpos” VALUE=“23768”>
<PARAM NAME=“lxssstepsize” VALUE=“48062”>
<PARAM NAME=“lxrefpos” VALUE=“92237”>
<PARAM NAME=“instance” VALUE=“Histology06a”>
<PARAM NAME=“lyssstepsize” VALUE=“35892”>
<PARAM NAME=“lslideyrefpos” VALUE=“17177”>
This browser does not support Java v1.1 applets!
</APPLET>

The interaction of this viewer with the server is also shown in FIG. 22. This viewer is simpler, and used for different purposes than the browser, but uses many of the same techniques of transferring image tiles.[0135]

FIG. 34 illustrates the layout and features of the HTML portal window created by this applet. This viewer consists of two views; a low-magnification view (which is the Preview Slide image discussed above) shown as an upper portion in FIG. 34, and a higher-magnification view shown in the lower portion. The two views are separated by a menu bar with four magnification choices. As described below, there is an HTML applet creation process which is another browser tab portion. This enables the creation of both the HTML code to generate a Java applet request and additional pre-configured images for the applet to use when it runs.[0136]

In an application of interest for this type of viewer, specific regions are identified in the image which are of primary interest, and the need is to see this region as quickly as possible and to change between magnifications rapidly. In order to enable this the applet creation process enables the location of a specific view on a given image, i.e., it specifies a center x, y position for the region and specifies a final view window size, of the same size as the lower portion of the portal window, and assembles from the tiled data structure four zoom level views corresponding to the menu bar magnification options. The zoom levels start with the highest Field View magnification level, usually 40× or 20×, and the viewer creates a lower-magnification image of each tile by using every other pixel at each lower zoom magnification. Additional tiles are brought in and assembled from the image data structure as needed to fill in the fixed field size of the lower HTML portal window. These four assembled images are referred to as Preview images, are given specific names in the creation process and are stored in a file accessible to the server program, on the same computer that the related image is located.[0137]

The first thing the Java applet does then after it is loaded is to send a Login and Virtual Slide Request as indicated in Table 1. If the slide name and server identity is correct, the server response is to send the Preview Slide image for the upper panel, the four Preview images that will be used for the lower panel, and the x, y list of all image tiles in the associated data structure. The HTML applet generation process specified which of the magnification choices would be loaded first. The other are available to the applet through the radio button event generated from the menu bar.[0138]

The advantage of this approach, of using the pre-stored Preview Slide and Preview images, is that they are small and can be transmitted relatively rapidly, essentially only five tiles, and are in essence pre-cached, in terms of the relationship to the browser description. One problem with applets is that they are interpreted rather than compiled; hence, they are slower than native machine code such as that used in the browser. Thus, this approach helps to overcome that. In addition, for many purposes, e.g., in an educational setting, these views are all that are needed to achieve the initial purpose. For the presentation of a microscope specimen, especially in anatomic pathology or histology, an overall view of the specimen, such as that shown in the upper portion, and localization of a specific region, with the ability to zoom in and out is sufficient.[0139]

The virtual slide link is set forth in Table 10 below.[0140]

	TABLE 10


	[WebSlide Link]
	tWebSlideURL=http://209.100.40.94/
	iMainTop=0
	iMainLeft=0
	tScanFilename=Prost-z2
	iMainOverlays=1
	bGraticles=1
	bScanArea=1
	bMultiMag=1
	bTileLoction=0
	bSlideView=1
	bFieldView=1
	iSlideViewTop=0
	iSlideViewLeft=600
	iSlideViewHeight=478
	iSlideViewWidth=1000
	iSlideViewWindowState=1
	bDisplayTileLocationOverlay=1
	iSlideViewZoomLevel=1
	lSlideXRefPos=44397
	lSlideYRefPos=55668
	iFieldViewTop=478
	iFieldViewLeft=0
	iFieldViewHeight=402
	iFieldViewWidth=472
	iFieldViewWindowState=1
	iFieldViewZoomLevel=1
	lFieldViewXRefPos=58436
	lFieldViewYRefPos=55520
	tSlideScanMode=0

In order to perform the multiheaded microscope function of emulation, a plurality of clients are logged on, which might include a client A and a client B. After having logged on, client B elects to consult with logged on client A and highlights client A's name in logged on list in a[0141]

step

800, as shown in FIG. 35A. The client B then selects a synchronization and user function by clicking on the sync on user button and a thin client browser enters a synchronization state keyed on signals from client A in astep802.

During the one-second interval update command for the browser, client B monitors client A's update state variables, as set forth in the listing in Table 6, and uses the variables necessary to display the same location and magnification of the slide data set that client A is currently viewing. A plurality of the state variables include state variable values that indicate whether those variables are disabled, for instance 999999999. Otherwise, the variable state is considered to contain active data and, during the one-second interval update, decisions are made by the state variables by client B, as set forth in[0142]

step

804. Control is then transferred to astep806 to determine whether the chat messenger index on the server is greater than the current state variable index. If it is, control is transferred to astep808 to request each missing chat message from the server and displayed in the chat window at the client until the chat message index on the server is equal to the state variable index following which the routine returns in astep810 to a test in astep812 to determine whether the state variables have been placed in sync mode. If they have not, control is transferred back to thestep806, as shown in FIG. 35D.

If the system is in sync mode, a test is made in a[0143]

step

814, as shown in FIG. 35A, to determine whether the virtual slide image selected from the slide tray data collection is the same as the one that is currently displayed. If it is not, the position in the slide tray is updated in astep816. If it is, control is transferred either from

step

814 or816 to astep818 where a test is made to determine whether the low-magnification x, y position location state variables are in the disabled state. If they are, control is transferred back tostep814. If they are not, the slide view window is displayed and updated for the low-magnification view to the lower-magnification position previously selected by client A using client A's current magnification state variable instep820 in order to synchronize the views.

A test is then made in a[0144]

step

Control is then transferred to a[0145]

step

830, as shown in FIG. 35C, where a test is made to determine the mouse pointer or display pointer x, y position state variables in the disabled state or not. If they are not disabled, the pointer is displayed at the Location selected by client A and control is transferred to step814. If the state variables are disabled, control is transferred directly to step814.

It should be appreciated that the updating function from the client A variables may take place not just with one client, client B but over multiple clients in order to provide image coherency from the client, in this example client A, which in effect controls the command token for the virtual multiheaded microscope remote emulation.[0146]

While there has been illustrated and described a particular embodiment of the present invention, it will be appreciated that numerous changes and modifications will occur to those skilled in the art, and it is intended in the appended claims to cover all those changes and modifications which fall within the true spirit and scope of the present invention.[0147]